Sr Site Contract Specialist - Fluent French Required - Sponsor Dedicated

Syneos Health

Not specified
Fluent french language required
Clinical trial contract management experience
Experience in cro or pharmaceutical industry
Syneos Health is seeking a Sr Site Contract Specialist fluent in French to manage contract processes for clinical trials. The role requires extensive experience in contracts management within the pharmaceutical industry, alongside strong project management and negotiation skills

Job Summary

  • The role involves administering all contract management processes including coordination with protocol, informed consent, and investigator documents at a project level.
  • Syneos Health is committed to building an inclusive culture where colleagues can authentically be themselves while driving impact for patients.
  • Candidates will support multi-country projects by negotiating and preparing contracts, budgets, and related documents for participation in industry-sponsored clinical trials.

Matching Summary

Match Score: 85

Syneos Health is seeking a Sr Site Contract Specialist fluent in French to manage contract processes for clinical trials. The role requires extensive experience in contracts management within the pharmaceutical industry, alongside strong project management and negotiation skills.

Skills & Requirements

Must-have

  • Fluent French language required
  • Clinical trial contract management experience
  • Experience in CRO or pharmaceutical industry
  • Knowledge of ICH GCP and clinical protocols
  • Strong negotiation and vendor management skills

Nice-to-have

  • Ability to mentor and train junior staff
  • Project management in fast-paced environments
  • Creative problem-solving for process improvement
  • Cross-functional collaboration with legal and finance
  • Commitment to inclusive culture and diversity

Key Requirements

  • BA/BS degree in Business Administration or related field
  • Advanced degree preferred
  • High level of contracts management experience
  • Essential experience in CRO or pharmaceutical industry
  • Excellent understanding of clinical trial start-up processes

Work Rights

Not specified

Sponsorship: required

Tailored Resume

Cover Letter